Method for Measuring a Bulbocavernosus Reflex

ABSTRACT

A system and method is disclosed for measuring muscle reflexes (e.g., a bulbocavernosus reflex) as a tool for identifying/diagnosing dysfunctions (e.g., spinal cord abnormalities, bladder voiding dysfunction, and sexual organ dysfunction) non-invasively by using mechanical stimulation. The system and method includes a probe having a predetermined patient contacting portion, wherein when the contacting portion is moved into contact with a particular area of the patient (e.g., the patient&#39;s genitals), the contact induces a muscle reflex. The probe detects the pressure resulting from the contacting portion being abruptly and forcibly brought into contact with the particular area. Such detection is used to electronically initiate capture of electrical responses from a plurality of electrodes placed on the patient&#39;s skin in proximity to the particular area. Such electrical responses are processed to determine characteristics of the patient&#39;s reflexes of one or more muscles adjacent to the electrodes.

RELATED APPLICATIONS

The present application is a continuation of U.S. patent application Ser. No. 12/324,726 filed on Nov. 26, 2008, which is a continuation-in-part of U.S. patent application Ser. No. 12/238,433 filed Sep. 25, 2008 which claims the benefit of U.S. Provisional Patent Application No. 60/975,056 filed Sep. 25, 2007, each of the above-identified applications is incorporated by reference herein in its entirety.

RELATED FIELD OF THE INVENTION

The present disclosure relates to obtaining and processing data indicative muscle reflexes for screening and/or diagnosing a patient, and especially for obtaining and processing data indicative of reflexes from the bulbospongiosus muscle. In particular, the present disclosure describes a novel electromechanical probe for stimulating the bulbospongiosus muscle, and consequently identifying a time of the stimulation so that electrical responses from electrodes on the patient's skin can be identified for analysis.

BACKGROUND

The bulbospongiosus muscle is one of the superficial muscles of the perineum. This muscle is innervated by the deep/muscular branch of the perineal nerve, which is a branch of the pudendal nerve. This muscle has a slightly different origin, insertion and function in males and females. In both sexes, however, bulbospongiosus muscle is important to normal sexual function and feelings, as well as urinary function. In males the bulbospongiosus muscle contributes to erection, ejaculation, and the feelings of orgasm. In females bulbospongiosus muscle closes the vagina and contributes to the feelings of orgasm.

The bulbocavernosus reflex (BCR) is a distinct, automatic (reflex) contraction of the rectum (part of the bowel) that occurs when the tip of the penis (in a man) or clitoris (in a woman) is squeezed or stimulated. In more technical terms, the bulbocavernosus reflex is a multi-synaptic reflex, and measurements of this reflex can provide indications of various neurological abnormalities in and around the pelvic floor, and the lower spinal region of a patient. For example, the integrity of afferent and efferent segments through sacral spinal segments (S2-S4) and pudendal nerve may be determined by such BCR measurements. Additionally, several levels of BCR abnormalities have been reported in cases with impotence when cauda equina or conus medullaris lesions are present, or when neurogenic bladder related to polyneuropathy is detected. Such BCR abnormalities appear as no BCR response, a prolonged latency in BCR response, or a temporal latency dispersion occurring in repetitive measurements. Moreover, a BCR response, if prolonged, can be an indication of pelvic nerve damage in patients with pelvic floor disorders.

It is known to use measurements of the BCR for diagnosis and treatment of various pelvic floor disorders, including those disorders mentioned above. Such measurements may be collected from, e.g., urethral and/or anal sphincters after stimulation of the dorsal nerve of the penis or clitoris via activation of electrodes appropriately attached to a patient. Additionally, such measurements have been obtained using EMG (electromyogram) testing. The following references are fully incorporated herein by reference for further description of EMG and the use of electrodes for diagnosing patient disorders:

-   U.S. Pat. No. 6,047,202 which discloses an electrode and array     thereof for collecting surface electromyographic signals. -   D. Prutchi in the publication “A High-Resolution Large Array (HRLA)     EMG System” published September 1995 in Med. Eng. Phys., Vol. 17,     442-454. Prutchi describes a bracelet which may be wrapped about a     body limb and which contains 256 surface electrodes to record the     electrical activity of underlying muscles. The electrodes are     arranged in eight groups of thirty-two electrode linear arrays     directly connected to buffer boards in close proximity of the     electrodes. Further processing of the electrical signals is     performed to provide a desired signal analysis, in this instance     primarily being concerned with the bidirectional propagation of a     compound potential in a single muscle in the upper arm of a human     subject or a histogram of total power contribution from active     fibers in a subject muscle, both being presented in charted format. -   U.S. Pat. No. 5,086,779 to DeLuca, et al., describes a back analysis     system of plural electrodes coupled to a computer system for     processing the signals and to provide graphical representations of     results. DeLuca's invention relates primarily to isolating     particular muscle groups by the use of support and restraint devices     which limit the movement of the patient's torso in predetermined     patterns correlated to the desired muscle groups. DeLuca's electrode     array consists of separate electrodes individually placed at desired     locations on a patient's back. -   U.S. Pat. No. 5,058,602 to Brody describes a method of     electromyographic scanning of paravertebral muscles comprising     measuring electrical potentials bilaterally across segments of the     spine. Readings are categorized into different patterns which are     indicative of different muscular conditions. Brody suggests     equipment useful within his described techniques as an available EMG     scanner having electrodes spaced 2.5 cm apart and a computer     component, but provides few details on the equipment or an     indication of usefulness for isolating certain muscles or muscle     groups. -   U.S. Pat. No. 5,318,039 to Kadefors, et al., describes a method and     apparatus for detecting electromyographic signals, processing them     and providing an indication of the change of the signal from a     predetermined norm. Kadefors' electrode system comprises three     electrodes, one of which is a reference marker. This electronic     apparatus, in essence, includes a sample and hold function in which     current responses can be compared to earlier responses and an     indication provided based on the differences detected. -   U.S. Pat. No. 5,505,208 to Toormin, et al., describes a method for     determining the status of back muscles wherein EMG signals are     monitored from a number of electrodes placed in a pattern on a     patient's back, the activity of each electrode is determined and the     results stored. A database of results provides a standard from which     comparisons can be made to determine deviations or abnormalities, as     a device for the care and management of the patient's dysfunction. -   U.S. Pat. No. 5,513,651 to Cusimano, et al., describes a portable     electronic instrument for monitoring muscle activity, using standard     ECG electrodes and a computer for analyzing the detected signals.     The electrodes are applied individually at predetermined locations     and a range of motion device is employed to generate signals related     to a particular muscle group. Output plots are produced to provide     an indication of results, apparently in the form of printouts of     information reflecting any deviations from the norm of expected     muscle activity.

Additional prior art references describing the use of the bulbocavernosus reflex for assessing patient dysfunctions are as follows, these references being fully incorporated herein by reference as well:

-   Sarica Y, Karacan I, “Bulbocavernosus reflex to somatic and visceral     nerve stimulation in normal subjects and in diabetics with erectile     impotence”, Journal of Urology, July 1987; 138(1): 55-8; -   Ertekin C, Akyurekli O, Gurses A N, Turgut H, “The value of     somatosensory-evoked potentials and bulbocavernosus reflex in     patients with impotence”, Acta Neurol Scand., January 1985; 71(1):     48-53; -   Ziemann U, Reimers C D. “Anal sphincter electromyography,     bulbocavernosus reflex and pudendal somatosensory evoked potentials     in diagnosis of neurogenic lumbosacral lesions with disorders of     bladder and large intestine emptying and erectile dysfunction”,     Nervenarzt, February 1996; 67(2): 140-6; -   Lavoisier P, Proulx J, Courtois F, De Carufel F, “Bulbocavernosus     reflex: its validity as a diagnostic test of neurogenic impotence”,     Journal of Urology, February 1989; 141(2): 311-4; -   Vodusek D B, Janko M, Lokar J., “EMG, single fibre EMG and sacral     reflexes in assessment of sacral nervous system lesions”, Journal of     Neurological Neurosurgery Psychiatry, November 1982; 45(11): 1064-6.

However, prior art procedures and apparatuses for obtaining such BCR measurements have been less than satisfactory, e.g., in their ease of use, and the discomfort caused to patients. Accordingly, it would be advantageous to have a non-invasive method and system for accurately detecting characteristics of the BCR response, such as latency in response, lack of response, abnormal reflex contractions, wherein such characteristics of the BCR are correlated with likely physiological and/or neurological dysfunctions.

SUMMARY

A system and method is disclosed herein for measuring muscle reflexes (e.g., a bulbocavernosus reflex) as a tool for identifying/diagnosing dysfunctions such as spinal cord abnormalities (e.g., in segments S2 thru S4), bladder voiding dysfunction, and sexual organ dysfunction. In particular, the novel screening system and method (referred to as a “screening system and method” herein) disclosed herein provides a non-invasive measurement of the muscle reflex using mechanical stimulation. Such non-invasive mechanical stimulation is advantageous because it is less painful to the patient than prior art measurement techniques, and in certain instances easier to obtain reflex measurements than prior art techniques for measuring a patient's muscle reflexes. More particularly, a probe is provided that includes a predetermined contacting portion for contacting the patient, wherein when the contacting portion of the probe is moved into contact with a particular area of the patient (e.g., the patient's genitals), the contact induces a reflex in one or more of the patient's muscles. Thus, the contacting portion of the probe provides a mechanical stimulus for inducing the patient reflex. In one embodiment, the probe detects the pressure resulting from the contacting portion of the probe being abruptly and forcibly brought into contact with the particular area of the patient's skin, wherein such detection is used to electronically initiate the capture of electrical responses from a plurality of electrodes placed on the patient's skin in proximity to the particular area. Such electrical responses can then be processed to provide characteristics of the patient's reflexes of one or more muscles adjacent to the electrodes.

In one embodiment of the probe, the patient contacting portion is detachable from the remainder of the probe so that for different patients different patient contacting portions are used. That is, the probe may be reusable with a plurality of patients except for the patient contacting portion which is replaceable between patients. Moreover, the patient contacting portion (or the probe itself if it is non-usable with different patients) may include an electronic device and non-volatile data storage for identifying whether the probe can be used for the data capture (and subsequent processing) of electrical responses indicative of muscle reflex contraction.

In one particularly important embodiment, the screening system and method disclosed herein measures the bulbocavernosus reflex response in units of milliseconds when this reflex is induced from the activation of the bulbospongiosus superficial muscle of the perineum via mechanical stimulation of the clitoris or penis. The resulting reflex measurements may be used for detecting abnormalities in the BCR such as no BCR response, a prolonged latency in BCR response, a prolonged BCR response, or a temporal latency dispersion occurring in repetitive measurements. As indicated above, such BCR abnormalities may be indicative of various patient dysfunctions, such as spinal cord damage in segments S2 through S4, urinary voiding dysfunctions, and/or sexual organ dysfunctions (e.g., impotence).

In one embodiment of the novel screening system and method disclosed herein, a prolonged bulbocavernosus reflex (e.g., more than 45 milliseconds), or an excessive latency in reflex response (e.g., more than 45 milliseconds) is considered a sign of neurological disease and/or neurological dysfunction. For example, a prolonged BCR response can be an indication of pelvic nerve damage in patients with pelvic floor disorders. Accordingly, results from the present screening system and method can be used in diagnosis and treatment of pelvic floor disorders.

The system and method disclosed herein includes components for EMG (electromyogram) testing to determine nerve and muscle function as a result of mechanical stimulation. In particular, such components include electrodes for measuring the bulbocavernosus reflex. Such electrodes include a reference electrode and a pair of sensing electrodes. The reference electrode applies a small voltage (e.g., a range of 1.0 to 3.5 volts DC, but more preferably 1.25 volts DC) to the skin of a patient during, e.g., mechanical stimulation of the penis or clitoris, the pair of sensing electrodes is used to detect the actual bulbocavernosus muscle contraction or reflex due to the mechanical stimulation. In a first operation of the electrodes 2 and 4, the voltage applied by the reference electrode induces a small electrical current that is generally believed to be in a range of 5 microamperes to 9 microamperes, to flow through the patient's skin. This range in current is based on a presumed skin resistance of 1-10 meg-ohms, as well as the placement of the reference and sensing electrodes. In particular, in one preferred embodiment, the reference and sensing electrodes are pairwise separated by, e.g., ½ to 1½ inches (more preferably 1 inch) in an equilateral triangular pattern or another non-collinear arrangement. However, it is within the scope of the present disclosure that other voltages in addition to or alternatively to the 3.3 volts may be applied to the reference electrode. In particular, such reference voltages may be changed from one activation of the screening system and method to another activation.

In another embodiment of the operation of the electrodes 2 and 4, instead of the reference electrode 4 providing a current for flowing through the patient to the sensing electrodes 2, the reference electrode 4 is used to adjust the voltage potential of the patient. In one embodiment, the output from the DC voltage source 42 to the electrode 4 is adjusted to provide the reference electrode 4 with a voltage potential in a predetermined range such as ±1.25 volts. When the potential voltage at the reference electrode 4 is adjusted to such a predetermined range, the potential voltage of the patient (at least in the skin area of the muscle response being measured) will not vary substantially from this predetermined range. As one skilled in the art will understand, in order for the SEMG 35 to effectively determine voltage differences between the sensor electrodes 2, the voltages measured from the electrodes 2 must be within a predetermined range dependent on the particular electrical characteristics of the SEMG 35. Accordingly, since a patient may initially have an unacceptably wide range of voltage potentials (e.g., ±1,000 volts) due to, e.g., static electricity, and/or being in proximity to an electrical current generating source, this reference electrode voltage is determined by adjusting the electrical output of the DC voltage source 42 to insure the reference electrode 4 has a voltage within a predetermined range so that the voltages at the electrodes 2 can be expected to be within an acceptable range for the particular SEMG 35 being used. In one embodiment, the range of acceptable voltages to the SEMG 35 from the electrodes 2 is ±3.3 volts. In one embodiment, the sensing electrodes may be positioned on the patient's skin at the 9 O'clock and 3 O'clock position around the patient's rectum as shown in FIG. 2, wherein the sensing electrodes may be within, e.g., a range of one to two inches from the patient's rectum. Additionally, the reference electrode may be positioned on the patient's inner thigh, e.g., approximately four to eight inches from the patient's rectum.

In the first operation of the electrodes 2 and 4, the current induced to flow through the patient's skin (by activation of the reference electrode positioned as described above), in turn, causes a very small voltage potential to develop between the sensing electrodes. In the second operation the electrodes 2 and 4, a small electrical potential is generated by the muscle cells when these cells contract. Regardless of the which operation of the electrodes 2 and 4 is used, the small potential difference in voltage between the sensing electrodes is amplified to a usable level using an instrumentation amplifier, or an amplifier and a (high pass) filter combination. This circuit utilizes a standard surface EMG amplification circuit with a gain of 6174.72, and then summed (mixed) with some portion of the amplified potential difference between the sensing electrodes.

An embodiment of the screening system and method may also include one or more diagnostic computational models for receiving analytical information generated from the signals output by the sensing electrodes, and, e.g., an indication of patient symptoms for determining one or more likely patient diagnoses. In particular, such models may receive the following analytical information: no BCR response, a prolonged latency in BCR response, a prolonged BCR response, a temporal latency dispersion, an amplitude of the BCR, an integral of a graph of the BCR, etc.

Moreover, it is within the scope of the present disclosure that an embodiment of the screening system and method may be utilized for receiving and analyzing electrical signals indicative of reflexes from other patient bodily areas, such as the knee (patellar reflexes), and intravaginal stimulation.

Additional features and benefits of the present disclosure are disclosed in the accompanying figures and description hereinbelow. Such additional features and benefits, to the extent they are novel and non-obvious, are considered a proper subject matter for patent protection regardless of where their disclosure is provided in this Summary section.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows an embodiment of the novel screening system and method disclosed herein. In particular, FIG. 1 shows the high level components of the novel apparatus for obtaining BCR measurements from electrodes (not shown) that are to be placed on a patient, wherein an exploded view of the probe 10 is shown.

FIG. 2 shows one arrangement of the sensing electrodes 2 and the reference electrode 4 on a female patient for obtaining electrical signals for measuring BCR by the novel screening system and method disclosed herein.

FIG. 3 shows the components of another embodiment of the novel screening system and method, wherein an exploded view of the probe 10 a is shown.

FIG. 4 shows the embodiment of FIG. 3 with the probe 10 a fully assembled.

FIG. 5 shows an output screen for viewing BCR measurements, in particular, the following are shown: the magnitude and location of the applied stimulus (via the probe 10), the magnitude and time for a time series of responses to the stimulus, the time delay between the application of the stimulus and corresponding response(s).

FIG. 6 shows a block diagram of another embodiment of the screening system and method disclosed herein.

FIG. 7 shows another embodiment of the probe (10 b) which may be used with a variation of the BRS module 108 shown in FIG. 6, wherein the identification chip 112 is not necessary to prohibit reuse of the probe with different patients.

FIGS. 8A and 8B show a different embodiment of the probe 10 b for supplying BCR signals to the BRS module shown in FIG. 6. In particular, a non-reusable probe tip cap 176 is shown (in cross section in FIG. 8A) which can be attached to the probe 10 b. The probed cap 176 contacts the patient and not the probe itself. Thus, the probe 10 b can be reused with different patients. Note that FIG. 8B is an end view of the probe 10 b and cap 176 combination as viewed from the patient contacting end of this combination.

FIGS. 9A and 9B show another embodiment of a probe (10 c) and a corresponding probe tip cap (176 c) for supplying BCR characteristic signals to a variation of the BRS module 108 shown in FIG. 6. Note that FIG. 9A shows a cross section of the cap 176 c, and FIG. 9B shows an end view of the probe 10 c and cap 176 c combination as viewed from the patient contacting end of this combination.

FIG. 10 illustrates one technique for preventing reuse of the cap 176 c, wherein mating slanted teeth (212 c and 216 c) engage for substantially assuring that once the patient contact shield 196 c contacts a patient for inducing a BCR, the cap cannot be reused. Note that the dashed representation of the patient contact shield 196 c as a disk is for simplicity of representation.

FIG. 11 shows a flat spring 220 c attached to the shaft 188 c, wherein the spring is also used to substantially assure that once the patient contact shield 196 c contacts a patient for inducing a BCR, the cap cannot be reused.

FIG. 12 shows an embodiment of the cap 176 c, wherein both the mating slanted teeth (212 c and 216 c) and flat spring 220 c are used to substantially assure that once the patient contact shield 196 c contacts a patient for inducing a BCR, the cap cannot be reused. In particular, this figure shows the flat spring 220 c in a compressed configuration. Note that the dashed representation of the patient contact shield 196 c as a disk is for simplicity of representation.

FIG. 13 illustrates the cap 176 c of FIG. 12. However, in FIG. 13 the flat spring 220 c is uncompressed, and accordingly prevents reuse of the cap 176 c for obtaining signal characteristics of a BCR. Note that the dashed representation of the patient contact shield 196 c as a disk is for simplicity of representation.

FIG. 14 shows another embodiment of the cap 176 c, wherein the flat spring 220 c is configured to also maintain the patient contact shield 196 c in position for the contacting the patient when the spring is in a compressed configuration. Note that the dashed representation of the patient contact shield 196 c as a disk is for simplicity of representation.

FIGS. 15A and 15B show another embodiment of a probe (10 d) and a corresponding probe tip cap (176 d) for supplying BCR characteristic signals to a variation of the BRS module 108 shown in FIG. 6. Note that FIG. 15A shows a cross section of the cap 176 d, and FIG. 15B shows an end view of the probe 10 d and cap 176 d combination as viewed from the patent contacting end of this combination.

FIG. 16 is an exploded view of one embodiment of the present invention.

FIG. 17 a is a top perspective view of one embodiment of the present invention.

FIG. 17 b is a perspective view of one embodiment of the present invention.

FIG. 17 c is a side perspective view of one embodiment of the probe of the present invention.

FIG. 18 is a further perspective view of a related embodiment of the present invention.

FIG. 19 is a further perspective view of a related embodiment of the present invention.

FIG. 20 is a perspective view of an embodiment showing a longitudinal axis.

DETAILED DESCRIPTION

The screening system and method disclosed herein includes mechanical stimulation of the penis or clitoris performed by a novel probe 10, wherein a first embodiment of this probe is shown in FIG. 1. In the embodiment of the probe 10 of FIG. 1 (shown in an exploded view), the probe includes a housing or handle 11, a piezoelectric disk or diaphragm 12, a stimulus plunger 13, a plunger housing 14, and a compression spring 15. When the probe 10 of FIG. 1 is assembled, the shaft 18 (of the stimulus plunger 13) extends through the bore or opening 22 of the plunger housing 14; however, since the expanded portion 24 of the stimulus plunger 13 can not fit through the opening 22, this prevents this plunger from sliding out the opening 22. The piezoelectric disk 12 seats against a stop 26 within the generally cylindrical interior of the housing 11. The compression spring 15 biases an opposing end 30 of the stimulus plunger 13 away from contact with the piezoelectric disk 12. The piezoelectric disk 12 is electrically activated by a power source that may be internal or external to the probe 10. FIG. 1 shows an embodiment of the probe 10 wherein there is a battery 17 within the housing 11 for energizing the disk 12 in a conventional manner as one of ordinary skill in the art will understand. Additionally, there is an electrical conductor 19 in the probe 10 between the disk 12 and an external electrical conductor 38, wherein signals indicative of the opposing end 30 contacting the disk are conducted by the conductors 19 and 38 for amplification and establishing a commencement of data capture from the electrodes 2 as will be described in further detail hereinbelow. Note that the use of a piezoelectric disk may be important to embodiments of the probe 10 over other mechanisms for detecting when to commence data capture from the electrodes 2 since a piezoelectric disc has a very quick response time that is required due to the very brief response times encountered by the BCR (e.g., generally less than 200 milliseconds).

At a very high level, the probe 10 is used to contact the patient's clitoris or penis and in particular, a probe tip 34 (referred to more generally hereinabove as a “patient contacting portion”) contacts the patient's clitoris or penis for thereby inducing a patient reflex response. The detection of the probe tip 34 contacting the clitoris or penis is accomplished by the probe 10 outputting an electrical signal indicative of the stimulus plunger 13 contacting the piezoelectric disk 12. The BCR in response to such contact is then detected by electrical signals output from properly positioned electrodes 2 on the patient's skin. Subsequently, such signals are amplified and then analyzed for determining/identifying characteristics of the amplified signals (and/or a graph thereof), wherein such characteristics may be used for identifying patient ailments and/or providing a patient diagnosis.

The compression spring 15, and plunger housing 14 restrain the stimulus plunger 13 in such a way that it can only move along the axis 16, and in particular, towards the piezoelectric disk 12 when the stimulus plunger tip 34 comes in contact with another object (e.g., a patient) with sufficient force to overcome the opposing force of the compression spring 15. Accordingly, when the stimulus plunger tip 34 comes in contact with a patient with such force so that the stimulus plunger 13 comes in contact with the piezoelectric disk 12 (while the disk is electrically activated), the disk distorts its shape (e.g., bends), and the mechanical stress caused by the stimulus plunger 13 contacting the piezoelectric disk 12 causes an electrical charge to develop on the surface of the piezoelectric disk 12. Since the disk 12 is electrically connected to an amplifier 36 (via the connection 19 and the external conductor 38), the electrical charge induced on the disk is detected by the amplifier for amplification (and at least in some embodiments, filtered as well via a high pass filter). Thus, the disk 12 functions as a sensor for detecting contact between a patient and the tip 34. However, alternative sensors may be used to detect the transfer of pressure from the tip 34 to the disk 12. In particular, the opposing end 30 may include a pressure sensitive switch (not shown) for detecting contact with the disk 12.

In one preferred embodiment, the probe 10 may be handheld by an operator for placing the probe in contact with a patient's penis or clitoris for initiating bulbocavernosus reflex. Moreover, in one preferred embodiment, the contact of the probe tip 34 with the patient's clitoris or penis is performed by an abrupt, non-invasive, pressure inducing motion that is preferably somewhat unexpected by the patient. Such a motion may be similar to inducing patellar reflexes during an examination of a patient's knee reflexes.

A battery 17 (e.g., internal to the probe), or a transformer (e.g., external to the probe, and not shown) may be used to electrically activate the disk 12 for detecting contact by the end 30 when genital simulation is performed via contact with the tip 34 of the shaft 18 (which extends through the bore 22).

Although such piezoelectric disks 12 may generate mechanical or pressure vibrations (i.e., oscillations in directions coincident with axis 16, FIG. 1), when electrically activated, wherein such vibrations may be transmitted to the tip 34, in at least some embodiments of the probe 10, any such vibrations are of substantially no consequence in inducing the genital stimulation. Said another way, the piezoelectric disk 12 is used only as a sensor for detecting the movement of the tip 34 when it contacts the patient for genital stimulation. However, additional/alternative methods of inducing such a BCR is also within the scope of embodiments disclosed herein. For example, the probe tip 34 may be vibratory such that the tip may first come in contact with the patient's clitoris or penis, and then commences a vibratory motion, wherein at the commencement of the vibratory motion, the probe 10 may output a signal indicative of the commencement of the vibratory motion. In particular, such contact prior to the on set of the vibratory motion may be relatively gentle and non-abrupt. It is believed that such vibratory motion may be provided by a piezoelectric disk 12 of appropriate manufacture.

The amplifier 36 (e.g., an EMG amplifier and high pass filter) amplifies the detected charge on the disk 12 induced by genital stimulation. The amplifier 36 responds by outputting a corresponding amplified response signal on the transmission cable 44 for transmission to a computer 40. The computer 40 is programmed to receive the probe 10 amplified signal as input, and assuming an electrical potential is being concurrently applied to the reference electrode 4 (e.g., via the DC voltage source 42), the amplified probe signal on the cable 44 act as a trigger to activate a signal conversion process 48 for commencing to sample the amplified electrode 2 signals output by the amplifier 36 via the surface electromyography (SEMG) unit 35. The computer 40 then converts the amplified signals from the electrodes 2 into a time series of numbers representing the magnitudes of the samples. In particular, the amplified electrode signals output on connection 46 a are amplifications of the differences of signals derived from the sensing electrodes 2 (FIGS. 1 & 2) on wires 46 b. In particular, the SEMG 35 receives the voltage signals from both of the electrodes 2 and forms a difference signal that is output to the amplifier 36. As shown in FIG. 2, the sensing electrodes 2 may be placed at predetermined locations on a patient's body, e.g., at the 9 and 3 O'clock positions around a patient's rectum. Additionally, the reference electrode 4 may be positioned as also shown in FIG. 2 (e.g., in the patient's crotch area nearer to the genital area than the electrodes 2), or in some embodiments, the reference electrode 4 may be positioned on the patient's inner thigh (e.g., within six inches of the patient's genital area, and more preferably within 4 inches).

Note that the probe 10 (and in some embodiments, only the probe tip, as discussed in other sections hereinbelow) may be a single patient use device (i.e., non-reusable), e.g., the probe (or probe tip) is, in at least preferred embodiments, deactivated after it has been attached to the computer 40 for, e.g., an extended time period of such as 30 minutes. Such an extended time period gives an operator of the screening system and method ample time to obtain measurements of the bulbocavernosus reflex desired for the screening process. Note that when the probe 10 is battery powered such deactivation may be provided by a draining of the one or more batteries; e.g., once the probe is activated, current continues to flow from the one or more batteries until the batteries cannot power the probe. However, it is within the scope of the present disclosure that other methods of deactivating such batteries may be used, such as having an operator manipulate a deactivation switch that permanently disconnects the electrical power to the piezoelectric disk 12, or by providing an electronic timer in the probe 10 that activates with the first activation of the probe and deactivates the probe after a predetermined time has elapsed.

Amplified voltage signals derived from the difference of the signals output by the sensing electrodes 2 are provided to the computer 40, and in particularly, to the signal conversion process 48. The amplified voltage signals includes signals representative of the potential (voltage) differences between the sensing electrodes 2 as determined by the SEMG 35.

However, in an alternative embodiment, the wires 46 b may connect directly to the amplifier 36 for simply amplifying and outputting each of its input electrode 2 signals. In such an embodiment, the signal conversion process 48 computes values representative of the potential differences between the sensing electrodes 2. Note that the SEMG 35 is not required in this embodiment.

Using the output from the amplifier 36, the signal conversion process 48 performs an analog to digital conversion, wherein the signals on the connection 46 a are sampled, digitized, and then the digitized samples are input to a computational procedure for generating a time series of records (e.g., a series of measurement records) representing the magnitude of the amplified signals over a predetermined elapsed time. More specifically, for each sampling period, the connection 46 a is sampled, the obtained sample is used to determine a number in a predetermined range of, e.g., 0 to 4096, wherein the greater the number, the greater BCR, and wherein such numbers from different reference electrode voltages can be reliably compared, summed, averaged or otherwise combined if desired. Moreover, the values in this predetermined range may be then normalized to the range 0.0 to 1.0, as one of ordinary skill in the art will understand.

However, it is within the scope of the present disclosure that, instead of the resulting time series of BCR numbers being monotonic with the BCR, such numbers may be inversely related to the BCR. Accordingly, instead of 1.0 being indicative of a maximal BCR response as is computed in the steps above, 0.0 would be indicative of the maximal BCR response.

The time period between samplings may be, e.g., 1.0 millisecond, although alternative time periods that are smaller or larger are within the scope of the present disclosure.

In one embodiment of the screening system and method, an analog to digital converter separate from the computer 40 may receive the signals from the amplifier 36 for performing the signal conversion process 48.

However, regardless of where the analog to digital conversion is performed, subsequently the analysis process 60 described hereinbelow is performed.

The analysis process 60 may be instrumental in determining BCR patient data to be output to the display device 52 (FIG. 1), to a database (not shown), and/or to a report generator (not shown). In particular, the analysis process 60 may determine one or more of the following BCR related measures when provided with digital data output from the signal conversion process 48:

-   -   (a) a latency between the detection of the response signal on         cable 44, and commencement of the BCR signals from the         electrodes 2,     -   (b) a duration of the BCR signals from the electrodes 2,     -   (c) a value indicative of a magnitude or strength of the BCR,         and/or     -   (d) an attenuation in the magnitude or strength of the BCR         (e.g., in comparison to an expected magnitude or strength).         Additionally, as described hereinbelow, the analysis process 60         may also determine associations between, e.g., values such         as (a) through (d) immediately above, and likely a diagnosis of         a patient's symptoms.

In order to more fully describe the processing and output of the analysis process 60, a description of a representative embodiment of output 56 (FIG. 1, and more particularly FIG. 5) from the analysis process is now described, wherein this output 56 is provided to a computer display device 52 operatively connected to the computer 40. In particular, referring to FIG. 5, a graph 62 may be displayed, wherein the horizontal (X) axis is elapsed time (in milliseconds), and the vertical axis represents signal magnitude values (preferably normalized to the range 0.0 to 1.0). A time value identified by the vertical line 64 on the graph 62 represents the detected application of the patient stimulus from the probe 10 as determined from the response signal on the cable 44. A subsequent time is identified by the vertical line 66 which represents the initial onset of the BCR in response to this stimulus. The Y (vertical) axis of the graph 62 represents the magnitude of a detected muscle (BCR) contractions. This magnitude is normalized in the range of 0.0 to 1.0 with 1.0 being the highest magnitude. The time series of normalized BCR response numbers is represented by the graphical signature 68. The horizontal line 72 is a reference line to facilitate viewing the graph 62. The auxiliary trace 74 is also for operator reference as well. In particular, the trace 74 provides the operator with a visual indication of all changes in voltage signals received from the electrodes 2 and the probe signals received on cable 44, wherein each change is shown by an upward movement in the trace 74. The values of the trace 74 may be computed as follows: Y_(n)=X_(n)·G where G=1/4096, and X_(n) is the n^(th) BCR response value, and Y_(n) is the normalized representation of the incoming time series, X_(n) is the input signal, G is the constant and n is the time start to stop.

In one embodiment, the position of the line 66 is manually assigned by an operator, wherein, e.g., the operator is able to set (and/or select and drag) this line to the position the operator determines is most indicative the onset of the BCR. However, in an alternative embodiment, the position of the line 66 may be estimated by the screening system and method, e.g., by identifying an initial time where the graphical signature 68 remains above a predetermined threshold for a predetermined elapsed time.

A patient symptom can be entered in the interaction box 76, and the collected patient data, and/or measurements/characteristics derived therefrom, can be associated with this symptom. Accordingly, once an actual diagnosis of the cause of the symptom is determined for each of a plurality of patients, associations may be obtained between: (i) such actual diagnoses, and (ii) the symptoms and corresponding measurements/characteristics of the collected patient data (e.g., patient graphical signatures 68). In particular, such associations may become the basis for one or more predictive models for predicting a likely (if any) patient abnormality/diagnosis, wherein such associations may be formed by one or more of: a statistical method (e.g., a regression technique), a learning system (e.g., a vector machine, and an artificial neural network), and/or a pattern matching system (e.g., a fuzzy logic system, etc.). In particular, it is believed that such associations may be based substantially on the symptom identification together with one or more of the following BCR measurements:

-   -   (a) a latency between the graphical signature 68 (equivalently,         the BCR signals from the electrodes 2), and the detection of the         response signal on cable 44,     -   (b) a duration of the graphical signature 68 (equivalently, the         BCR signals from the electrodes 2),     -   (c) a magnitude of the graphical signature 68 (equivalently, the         BCR signals from the electrodes 2),     -   (d) an attenuation in the magnitude of the graphical signature         68 (equivalently, the BCR signals from the electrodes 2),         wherein such attenuation is, e.g., in comparison to an expected         magnitude, and/or     -   (e) no detectable graphical signature 68 (equivalently, the BCR         signals from the electrodes 2).

Alternatively/additionally, the resulting time series of the digital data stream from the signal conversion process 48 can be input to an embodiment of analysis process 60 for hypothesizing a diagnosis for (any) one or more of sexual, lower spinal, and/or urological dysfunctions. Such hypotheses may be generated by one or more hypothesis generating predictive models which are described hereinbelow.

Of course, if none of the models identify a likely diagnosis, then it may concluded that the patient is not likely to have dysfunctions, such as sacral cord lesions, or prudential neuropathy (impotence, chronic back pain, fecal incontinence) resulting from lack of sacral plexus integrity.

In one such predictive model, a prolonged bulbocavernosus reflex of more than 45 msec., such as is shown in FIG. 5, may be considered indicative of a neurological disorder. More precisely, such a model may hypothesize one of the following disorders: sacral cord lesions, prudendal neuropathy (impotence, chronic back pain or disc disease), and lesions of the cauda equine. In one embodiment, prolonged such bulbocavernosus reflexes are determined by a calibration or training process, wherein time series BCR data is obtained from patients with such neurological disorders, and such data is used for determining parameters indicative of such disorders.

Additionally, such a model (or another model) may also identify an abnormal BCR latency, wherein such latency (e.g., in a range of 50+ msec.) may be indicative of the following disorders: diabetic neuropathy, or other, neurogenic disease process.

Moreover, such a model (or another model) may also provide output corresponding to an indication of a substantial absence or attenuation of the BCR within the predetermined sample time period for sampling the signals from the electrodes 2. In particular, such BCR absence or attenuation may be indicative of the following symptoms: sexual dysfunction, voiding dysfunction, and bowel dysfunction. Accordingly, the following may be considered likely diagnoses: decreased or absent sacral plexis response. Note that attenuation of the BCR in a graphical signature 68 also may be quantified as no bulbocavernosus response, particularly if such attenuation is below, e.g., a predetermined threshold such as a threshold corresponding to 2 micro volts above a baseline output from the muscle(s) at rest.

There are numerous measurements related to the graph 62 that may be determined to be effective for predicting patient disorders (i.e., diagnosing a patient's symptom(s)), and various calibration or training processes may be used to determine the measurements that are most effective in providing an appropriate diagnosis. In addition to the measurements/characteristics of the BCR patient data received from the signal conversion process 48, some additional measurements that may be useful in diagnosing a patient's symptoms are: the integral of the graphical signature 68, the number or magnitude of local minima or maxima, an extent of the graphical signature 68 below/above a predetermined value, etc.

In one embodiment of the presently disclosed system and method for screening, instead of (or in addition to) hypothesizing/diagnosing various disorders/symptoms, any of the above mentioned statistics or characteristics of the graphical signature 68 may be computed from the BCR digital data streams, and then output to a technician, nurse or physician for review and interpretation.

In one embodiment of the screening system and method, one or more of the following assessments may be obtained from analysis of the BCR time series measurements generated by the signal conversion process 48:

-   -   (a) the patient's spinal cord segments S2 through S4 are in         tact,     -   (b) there may be lesions in the cauda equine,     -   (c) an indication of actual chronic back pain, e.g., as asserted         by the patient,     -   (d) the latency between genital stimulation and the resulting         bulbocavernosus reflexes are within a normal range and are not         indicative of neurological order (e.g., contrary to what is         asserted by the patient),     -   (e) the latency between genital stimulation and the resulting         bulbocavernosus reflexes are abnormal and are indicative of         neurological order,     -   (f) the BCR time series measurement are indicative of a voiding         dysfunction, bowel dysfunction, and/or     -   (g) the time series measurements are indicative of a male         impotence condition.

A report may be generated by the analysis process 60, and the report can be printed for entry into the patient's medical records, wherein the report may include any of the information disclosed hereinabove.

Another embodiment of the probe is shown in FIGS. 3 and 4, wherein components that functionally correspond to components of probe 10 described hereinabove are identified by the same numerical label except with an “a” following. Accordingly, the probe is identified by the label “10 a”.

One or more of FIGS. 3 and 4 show:

-   -   (i) a handle 11 a for holding the probe 10 a,     -   (ii) a piezoelectric disk 12 a for at least detecting a         mechanical pressure from the tip 34 a for stimulating a         patient's penis or clitoris in a similar manner as discussed         hereinabove.     -   (iii) a stimulus plunger 13 a for transferring toward the         piezoelectric disk 12 a a resulting mechanical movement of the         tip 34 a contacting the patient's penis or clitoris; in         particular, the plunger 13 a includes the tip 34 a, and an         opposing end 30 a,     -   (iv) a plunger housing 14 a which is operatively attached to an         end of the handle 11 a for retaining at least part of the         stimulus plunger 13 a therein; note that as with the plunger         housing 14 of the probe 10, the plunger housing 14 a includes an         opening or bore 22 a through which the shaft 18 a of the         stimulus plunger 13 a extends, and the stimulus plunger 13 a (as         with the stimulus plunger 13) includes an expanded portion 24 a         that prevents the plunger from slipping entirely through the         opening 22 a,     -   (v) a compression spring 15 a for separating the stimulus         plunger 13 a from the piezoelectric disk 12 a; in particular,         the end 70 of the spring 15 a fits onto an end 74 of the         pressure transfer rod 78, and the spring end 82 contacts the         opposing end 30 a of the plunger 13 a within the channel 84         extending the length of the handle 11 a.

When the probe 10 a is fully assembled, the piezoelectric disk 12 a is sandwiched between washers 86 a,b (preferably plastic). The disk 12 a and washers 86 are contained within an interior 90 of the piezohousing 94 which is secured to the end 98 of the handle 11 a by, e.g., adhesive, mating threads, a snap fit, or another comparable securing mechanism. An endcap 102 seals the disk 12 a and the washers 86 a and 86 b within the interior 90 by, e.g., snapping the semi-annular locking projections 106 onto the ridge or recess 110 adjacent the opening 114 of the interior 90. Additionally retained in the interior 90 is a tapered compression spring 118 which provides a pressure on the piezoelectric disk 12 a at all times. When the pressure transfer rod 78 is positioned in the channel 84, the expanded head 122 rests against the center opening in the washer 86 a, but the expanded head is too large to fit through this opening.

During operation of the probe 10 a, an operator activates the probe 10 a by, e.g., a quick downward (preferably at least somewhat unanticipated) pressure of the stimulus tip 34 a on the clitoris or penis. In one embodiment, when electrical power is already being supplied to the disk 12 a from an electrical power source, e.g., a battery 17 a (preferably positioned between the disk 12 a and the washer 86 b) within the handle 11 a, or an exterior electrical power supply (not shown), such activation of the probe by contacting a patient's genital area causes the end 74 of the transfer rod 78 and the opposing end 30 a to come in contact (or otherwise become configured for the transfer of tip 34 a movement). Accordingly, the movement of the tip 34 a toward the interior of the plunger housing 14 a causes movement of the transfer rod 78 for increasing pressure on the disk 12 a, wherein such increased pressure results in an additional electrical charge to develop on the surface of the piezoelectric disk. Since the disk 12 a is electrically connected to the amplifier 36 (via a connection not shown, and the external conductor 38 a), the electrical charge induced on the disk is detected by the amplifier for amplification. Thus, the disk 12 a functions as a sensor for detecting contact between a patient and the tip 34 a. However, note that alternative embodiments of sensors may be used to detect the transfer of pressure from the tip 34 a to the disk 12 a. In particular, the opposing end 30 a may include a pressure sensitive switch (not shown) for detecting contact with the disk 12 a.

Alternatively, such activation of the probe 10 a by contacting a patient's genital area may initiate an electrical current from a power source (e.g., a battery 17 a, or an exterior electrical power supply) to the piezoelectric disk 12 a thereby causing the disk to apply vibratory pressure to the transfer rod 78 for initiation of the BCR reflex. Thus, when the tip 34 a is pressed against the penis or clitoris, the shaft 18 a slides further into the plunger housing 14 a and handle 11 a for thereby compressing the spring 15 a so that vibratory pressure from the disk 12 a results in mechanical vibrations being transferred to the tip 34 a (via the shaft 18 a and the transfer rod 78) for stimulation of the penis or clitoris.

As with the probe 10, at the time that the vibratory pressure commences to transfer to the tip 34 a, a mechanical stress caused by the head 122 applying additional pressure against the disk 12 a causes an electrical charge to develop on the surface of the disk. This electrical charge is communicated to the external conductor 38 a via an internal conductor (not shown), and subsequently conveyed to the amplifier 36 (e.g., an EMG amplifier) where it is detected, and amplified as described hereinabove. The amplified signal is transmitted to the computer 40 (via transmission cable 44) as also described hereinabove.

Accordingly, the probe (10 or 10 a) at least provides electrical signals for identifying when to commence measuring an electrical response (via the sensing electrodes 2) to a BCR.

In each of the above embodiments of the probe 10 and 10 a, the included disk (or other vibration generating element) may be selected for generating vibrations having frequencies in the range of 2 Hz to 20 Hz, and more preferably in the range of 4 Hz to 10 Hz, most preferably approximately 5 Hz. In particular, the inventors have determined that vibrations outside of these ranges have reduced effect on the patient, and/or may be painful.

Note that in addition to activation of the probe (10 or 10 a) by contacting a patient's genital area, the probe may include an activation switch (e.g., button switch 124, FIG. 3), wherein pressing (or otherwise manipulating) such a switch induces a current to flow to the disk 12 a for providing an electrical potential to the disk. Such a switch may only activate the electrical features of the probe, and not be capable of turning off such features. Accordingly, as described hereinabove, a battery powered embodiment of the probe may be used for only a prescribed time before becoming non-functional due to, e.g., one or more dead batteries. However, other mechanisms may also be used for prohibiting the reuse of the probe with another patient. For example, a deactivation timer may be incorporated into the probe.

Note that for embodiments of the probe wherein the included disk remains in a vibratory active state once the probe is powered on, such vibrations (or lack thereof) can be an indicator to an operator as to whether the probe has been previously used. For example, if upon activation of the activation switch, the operator senses no vibratory response from the disk 12 or 12 a (e.g., due to a dead battery, and/or due to detection that the activation switch has been previously used to power the probe, etc.), then the operator will be alerted that the probe is at least non-functional and may have been used previously.

Moreover, at least some embodiments, the probe (10 or 10 a) may include a light emitting diode to notify an operator that the probe has not been previously used. For example, for a functional probe that had not been previously activated, such a diode would be activated when the button switch 124 is pressed for electrically activating the probe, and such a diode would emit light until a predetermined probe state occurs that deactivates the probe and prevents the probe from being reactivated.

Embodiments of the probe (10 or 10 a) may also prohibit their reuse based not only on an elapsed time, but also on the number of times the probe tip is depressed toward the interior of the probe housing. For example, by providing no more than, e.g., five probe tip depression within a predetermined maximal elapsed time of probe activation, additional assurance that the probe will not be reused with another patient can be provided.

Referring now to FIG. 6, a more detailed diagram of an embodiment of the screening system and method is disclosed. The components (and communications therefor) described in FIG. 6 that have substantially identical functionality with components described hereinabove are identified by the number of the component described above followed by “x”. Moreover, an embodiment of the probe 10 x shown in FIG. 6 may be one of: probe 10 or 10 a, or another embodiment. The components, communications, and data processing of the embodiment of FIG. 6 are described in the following sections (1) through (7).

(1) Description of the Components Shown in the Embodiment of FIG. 6.

-   -   (1-1) A Bulbocavernosus Reflex Stimulation (BRS) External Power         Supply 104 is a medical grade power supply that is used to         supply 24 volt DC power to the BRS Module 108 (described         hereinbelow).     -   (1-2) A probe 10 x is used to administer and measure the genital         stimulation in a manner as described in previous embodiments         hereinabove. The tip 34 x in the probe 10 x may be replaceable         and may contain an ID chip 112. The ID chip 112 is used to         prevent its tip 34 x from being used more than once (e.g.,         prevented from being used on more than one patient) as is         described further hereinbelow. Thus, instead of the entire probe         10 x being non-reusable on different patients, only the probe         tip 34 x is non-reusable. The probe 10 x interfaces to the BRS         Module 108 (which includes an amplifier/filter 36 x having         substantially identical function to the combination of the SEMG         35 and the amplifier 36 disclosed in FIG. 1 and described         hereinabove). In particular, the amplifier/filter 36 x includes         a surface EMG amplifier/filter 116 for receiving signals from         the electrodes 2, and a stim(ulus) probe amplifier 120 for         receiving signals indicative of probe 10 x activation (via cable         38 x. Both amplifiers 116 and 120 are described hereinbelow.     -   (1-3) The ID chip 112 provided in the probe tip 34 x can output         data to the BRS module 108 for determining whether the probe tip         has been previously used to contact a patient, and if so, the         elapsed time since this first use. In one embodiment, such data         includes a time and date that the probe 10 x was first         activated, or if not previously used such data may include a         predetermined value such as zero. Thus, the ID chip 112 includes         a non-volatile data storage for storing data indicative of the         probe tip's activation history (which may be only the initial         date and time of, if any, the probe tip's first activation). In         one embodiment, such activation history may include the time and         date of each activation, and/or the elapsed time of each         activation. Note that the ID chip 112 may be activated each time         the probe 10 x is operably connected to the BRS module 108. In         particular, data is communicated on the conductors 160 a and 160         b from the MCU 128 processor (described below) for activating         the ID chip 112 so that it will respond to the MCU with an         acknowledgement of whether the probe tip 34 x can or cannot be         used for a subsequent patient contact. Accordingly, an         acknowledgement by the ID chip 112 that the probe tip 34 x         cannot be used will cause the MCU 128 to issue commands to at         least prevent data collection from the probe 10 x, and         preferably provide an indication to the operator that the probe         having this tip cannot be used for such data collection. There         are various ways to provide such an indication of probe non-use,         e.g., visual display on the BRS module 108 may be used such as a         red LCD may light when the probe cannot be used, and a green LCK         may light when the probe can be used. Alternative/additional         visual and/or auditory presentations are also within the scope         of the present disclosure. Accordingly, iconic and/or textual         information can be visually presented to an operator for         indicating whether the probe 34 x (with its current probe tip 34         x) can be operably used. Alternatively/optionally, synthetic         speech or various sounds may be used for indicating whether the         probe 34 x (with its current probe tip 34 x) can be operably         employed.     -   (1-4) The BRS Module 108 is the interface unit between the BRS         Computer 40 x and both the patient applied probe 10 x and EMG         leads (collectively labeled as 46 x in FIG. 6).         Subsystems/components of the BRS Module are as follows:         -   (1-4.1) Micro Controller Unit (MCU) 128.             -   The MCU 128 is a microprocessor that controls and                 monitors data and communication in the BRS Module 108.                 The MCU 128 contains firmware for the following                 functions:                 -   a. Connects and communicates with the BRS computer                     40 x via the USB interface 132.                 -   b. Upon command the MCU 128, collects digital data                     from the surface EMG analog to digit converter 136                     (which converts the amplified voltage differences                     from the electrodes 2 to digital data), and the Stim                     Probe analog to digital converter 140 (which                     converts the amplified probe activation signal to                     digital data). The MCU 128 then sends such digital                     data to the BRS computer 40 x via the USB interface                     132,                 -   c. Monitors the 24 volt power supply 104 and                     communicates the status of this power supply to the                     BRS computer 40 x via the USB interface 132.                 -   d. Reads and updates the IC chip 112 in the Stim                     Probe Tip 34 x to ensure that the Probe Tip is not                     used for more than 30 minutes.         -   (1-4.2) Isolation DC/DC Converters 144.             -   The Isolation DC/DC converters 144 supply isolated                 −3.3V, +3.3V, and 5V DC power to the patient connected                 components; in one embodiment such converters may be: a                 Datel UWR-5/2000-D24E-C Murata NDTD0503C or similar                 components as one of ordinary skill in the will                 understand.         -   (1-4.3) Isolation Barrier 148.             -   The Isolation Barrier 148 provides the necessary                 creepage and clearance distances between the AC mains                 connected power and patient connected power.         -   (1-4.4) Power Detector 152.             -   The power detector 152 is used by the microprocessor MCU                 128 to monitor the state of the 24 Volt Power supply                 from the power supply 104.         -   (1-4.5) Digital Optical Isolators 156.             -   The Digital Optical Isolators 156 are used to provide                 isolation between the patient connected electronics                 (i.e., the electrodes 2 and 4), and USB powered                 electronics (i.e., the computer 40 x). The optical                 isolators 156 allow the MCU 128 to communicate with the                 analog to digital converters 136 and 140, and the chip                 112 in the Stim Probe Tip 34 x via a one wire interface                 provided by the conductors 160 a and 160 b.         -   (1-4.6) Stim Probe Amplifier/Filter 120.             -   The Stim Probe Amplifier/Filter 120 amplifies and                 filters the signal from the Stim Probe 10 x to a level                 that can be read by the A/D converter 140. The MCU 128                 controls the analog to digital conversion process of the                 A/D converter 140.         -   (1-4.7) Stim Probe A/D (Analog to Digital) Converter 140.             -   The A/D converter 140 is an analog to digital converter                 for changing the incoming amplified Stim Probe 10 x                 signal into a digital value for the MCU 128 to read and                 then send to the computer 40 x for analysis. The MCU 128                 controls the A/D conversion process of the A/D converter                 140.         -   (1-4.8) Surface EMG Amplifier/Filter 116.             -   The Surface EMG Amplifier/Filter 116 amplifies and                 filters the voltage signals from the electrodes 2 to a                 level that can be read by the A/D converter 136.         -   (1-4.9) Surface EMG A/D (Analog to Digital) Converter 136.             -   The converter 136 is an analog to digital converter for                 changing the incoming amplified Surface EMG signal into                 a digital value for the MCU 128 to read and send to the                 computer 40 x for analysis.         -   (1-4.10) Signal Conditioner 164.             -   The signal conditioner 164 translates the two wire                 interface 160 a from the MCU 128 to/from the 1 wire                 interface 160 b which communicates with the ID chip 112.     -   (1-5) Computer 40 x.         -   The computer 40 x provides a user interface for displaying,             e.g., displays such as shown in FIG. 5 described             hereinabove. The computer 40 x communicates with the BRS             Module 108 through the USB interface 132. The computer 40 x             contains a custom application for at least the following             functions:             -   a. Communicates and receives status information from the                 BRS Module 108 regarding power on (more generally                 activation status), information for obtaining probe tip                 ID chip 112 information (e.g., BCR time series values,                 ID chip status, etc).             -   b. Sends commands to the BRS Module 108 to acquire data                 from the Stim probe 10 x.             -   c. Graphs and/or analyses data from the Surface EMG data                 channel (which includes the components 116, 136, 156,                 and 128), and from the Stim Probe data channel (which                 includes the components 10 x, 38 x, 120, 140, 156, and                 128) for presentation to an operator. The graphs and/or                 analysis performed may be as described hereinabove                 regarding the analysis process 60 (FIG. 1) and the user                 interface of FIG. 5.             -   d. Processes the Stim probe 10 x signal to determine the                 time of commencement of patient stimulation.             -   e. Allows an operator to input patient and physician                 information.             -   f. Stores test case data for later review and analysis.             -   g. Prints reports is instructed by an operator.     -   (1-6) Printer 168.         -   The printer 168 is used by the Computer 40 x to print             reports on patient cases.

(2) High Level Processing of Data in the BRS Module 108.

-   -   For each of the EMG data channel (which includes the components         116, 136, 156, and 128), and the Stim Probe data channel (which         includes the components 10 x, 38 x, 120, 140, 156, and 128) the         high level algorithm used to process incoming analog data can be         simplified down to:         -   (a) first inputting the analog data to an amplifier and a             high pass filter (provided by the components 116 and 120),             followed by a RMS detector process (provided by the A/D             converters 136 and 140), and         -   (b) providing the output from (a) immediately above to a             process (provided by the computer 40 x), wherein the data is             decimated down from a 2 KHz sample rate to a 1 KHz sample             rate by simply saving every other sample.     -   The signal provided by each of the above-identified channels         passes through its own filter and RMS detector and decimator         before being stored in the computer 40 x (or a database operably         connected thereto).     -   (2-1) Implementation.         -   Each high pass filter is implemented as a 4 pole Butterworth             filter having a cutoff frequency of 10 Hz and a pass band             ripple of 0%. Each RMS detector is implemented using the             Root Mean Square algorithm for a finite number of sequential             samples.

(3) Filter Algorithm

-   -   Each filter used in the amplifier/filter 36 x may be a Chebyshev         filter optimized for a pass band ripple of 0%, otherwise known         as a Butterworth filter. Each of the filter is a form of         recursive filter, which is also called an IIR (Infinite Impulse         Response) filter. For a detailed description of recursive         filters and the implementation see the Scientists and Engineers         Guide to Digital Signal Processing chapters 19 and 20, by         Steven W. Smith, published by California Technical Publishing     -   (3-1) Implementation.         -   Each of the filters utilizes an embodiment of the following             equation, as one of ordinary skill in the art will             understand.

y[n] = a₀x[n] + a₁x[n − 1] + a₂x[n − 2] + a₃x[n − 3] + … + a_(n)x[0] + b₁x[n − 1] + b₂x[n − 2] + b₃x[n − 3] + … + b_(n)x[0],

-   -   wherein for 0≦i≦n, a_(i) is the recursion coefficient of the         incoming signal, b_(i) is the recursion coefficient of previous         output signals, x[i] is the incoming signal, and y[i] is the         output signal.

(4) RMS Algorithm

-   -   The RMS (Root Mean Square) is a measure of the magnitude of a         varying quantity (e.g., a signal), which is calculated for a         series of discrete values for a continuously varying function.         The BRS software uses the RMS algorithm to transform the         incoming signals into a magnitude (as opposed to a wave) so that         the analysis by an operator easier. The period of the function         is configurable by the operator. For a more detailed description         of the RMS algorithm see http://en.wikipedia,org/wiki/Root_mean         square.

(5) Stimulation Marker Detector Algorithm.

-   -   The Stimulation Marker Detector algorithm scans the stimulation         probe time series (received via the cable 38 x) looking for a         change in signal amplitude of 1%±0.1% within a 50-millisecond         window. If/when a change in amplitude at t+50 that exceeds this         threshold is detected, a marker is placed in the data stream of         the Stim Probe data channel, wherein the marker corresponds to         time t. If a marker is detected, this algorithm is blacked out         for a period of 1.5 seconds.     -   (5-1) Implementation         -   For each sample in the time-record (minus 50 mS) perform the             following steps:             -   (5-1.1) Scan ahead of current position up to 50 mS;             -   (5-1.2) If the magnitude of the stimulus signal meets                 criteria, place a marker in the data stream of the Stim                 Probe data channel;             -   (5-1.3) Black out additional marker placement for 1.5                 seconds

From the disclosure hereinabove, and the accompanying figures, it is believed that one of ordinary skill could manufacture the present screening system, and in particular, the probe (10 and/or 10 a). More particularly, FIGS. 1 and 3 are believed to provide effective indications as to how the components of the embodiments of the probe would be assembled.

Other embodiments of the probe are shown in FIGS. 7 and 8A and 8B, wherein components that functionally correspond to components of probe 10 and/or 10 a described hereinabove are identified by the same numerical label except with an “b” following. Note that in each of the embodiments of FIGS. 7 and 8, a piezoelectric disk (12 or 12 a) together with the pressure transferring components (e.g., the stimulus plunger (13 or 13 a), the compression spring (15 or 15 a), and the pressure transfer rod 78) of the probe embodiments 10 and 10 a are not needed in the present embodiments of FIGS. 7 and 8A and 8B. Referring to the probe 10 b of FIG. 7, the probe tip 34 b includes two spaced apart electrodes 172 for conducting an electrical current therebetween during operation. In particular when the button 124 b is used to activate the probe 10 b, a low difference in potential voltage is provided between the electrodes 172, and this difference is used to generate a small current between these electrodes when the probe tip 34 b contacts the patient. In one embodiment, the operator of the probe 10 b may provide an electrical conducting gel (not shown) on the patient's genital area where the probe tip 34 b is to contact the patient. After application of the gel, the operator then contacts the genital area having the gel thereon for inducing a BCR response (the contact being, e.g., an abrupt, at least partially unanticipated genital contact of sufficient force to induce the BCR response). Accordingly, upon genital contact, a current between the electrodes 172 flows through the gel and can be used to capture data indicative of the time of contact at least as accurately as the embodiments of the probe 10 and 10 a described hereinabove. It is believed that there are numerous examples of such gels that may used during operation of the probe 10 b, e.g., Electrode Jelly by Mavidon located at 1820 2^(nd) Ave. No., Lake Worth, Fla. 3346, and/or Lectron II Conductive Gel.

Since the electrodes 172 may be fixedly attached to the tip 34 b, and this tip fixedly attached to the probe handle 11 b, the probe 10 b of FIG. 7 may have no moving mechanical parts during operation. Moreover, the diaphragm (12 or 12 a) of the previous embodiments as well as various shafts (e.g., 18 and 18 a) and springs (e.g., 15, 15 a, 118) are not needed in the probe 10 b.

Embodiments of the probe 10 b may be configured with various parameters. For example, the electrodes 172 may be spaced apart in a range of 1/16 of an inch to 7/16 of an inch. Additionally, the voltage difference between the electrodes 172 may be in the range of 0.25 Volts to 1.0 Volt, and more preferably from 0.3 Volts to 0.7 Volts. Note that any leakage of current from one of the electrodes 172 to the sensing electrodes 2 can be compensated for.

In the embodiment of FIGS. 8A and 8B, a deposable dielectric cap 176 can be provided over the tip 34 b, wherein the cap has spaced apart electrically conductive leads 180 wherein each such lead contacts exactly one of the electrodes 172. Accordingly, since the leads 180 extend through the thickness of dielectric material of the cap 176, upon use of the probe 10 b, the exterior conductive surfaces 184 of the leads will have the difference in voltage potential of the electrodes 172. Thus, when the surfaces 184 contact the conductive gel on the patient's skin, the current flowing (and/or the voltage difference drop) between the electrodes 172 can be detected in a similar manner as in the probe 10 and/or 10 a embodiments above for thereby determining a delay in the resulting (if any) BCR.

Note that the cap 176 may be secured to the embodiment of the probe 10 b (e.g., as shown in FIGS. 8A and 8B) by various techniques. In FIGS. 8A and 8B, the cap 176 has a circular ring 189 (having, e.g., a triangular cross section) projecting into the interior of the cap, wherein this ring snap fits into a corresponding circular detent 192 in the probe 10 b. In other embodiments, ring 189 need not be continuous around the probe 10 b, and may have a different cross section. Additionally/alternatively, alignment slots 192 may be provided in the probe 10 b (alternatively, the cap) for mating with corresponding projections 195 from the cap 176 (alternatively, the probe).

In one embodiment of the cap 176, a cap stabilizer 198 may include an ID chip 112 as described hereinabove. In particular, the ID chip 112 can be in signal communication with an electrical fitting 199 for communicating with the BRS module 108 as described hereinabove.

FIGS. 9A and 9B show another embodiment of a cap (176 c) together with another additional embodiment of the probe (10 c), wherein components that functionally correspond to components of previous embodiments of the probe or the cap 176 described hereinabove are identified by the same numerical label except with a “c” following. FIG. 9 shows cap 176 c for covering the probe tip 34 c, wherein this cap has a shaft 188 c which is slidable along axis 208 c within a bore 192 c through the cap 176 c. Fixedly attached to the shaft 188 c is an expanded portion 184 c (which may be a disk or washer fixedly attached to the shaft), wherein the expanded portion is symmetric around the shaft 188 c, and the axis 208 c is the axis of the shaft 188 c. A single electrical conductor 180 c (which may be a circular ring attached to the expanded portion 184 c, and concentric to the shaft 188 c) is provided. An outer end of the shaft 188 c is attached to a patient contact shield 196 c for contacting a patient's genital area and thereby inducing a BCR; the shield covers the tip 34 d, and according may be any of various shapes including hemispherical. An inner end of the shaft 188 c has attached thereto an elastomeric component 200 c such as a sponge-like material. The inner end of the shaft 188 c and the elastomeric component 200 c are received in a recess 204 c within the probe 10 c, wherein the shaft 188 c is slidable along the axis 208 c within the recess. Note that in the embodiment of FIGS. 9A and 9B, a piezoelectric disk (12 or 12 a) together with the pressure transferring components (e.g., the stimulus plunger (13 or 13 a), the compression spring (15 or 15 a), and the pressure transfer rod 78) of the probe embodiments 10 and 10 a are not needed in the present probe and cap combination. Moreover, as will be detailed more fully below, by taking of the advantages of one or more of the improvements shown in FIGS. 10-14, of an identification chip (112) may not be needed for limiting the reuse of the cap 176 c.

During operation of the probe 10 c with the cap 176 c operably attached thereto as in FIGS. 9A and 9B, the elastomeric (or spring) component 200 c fits within the closed end of the recess 204 c and exerts a force effective for causing the expanded portion 184 c to contact the interior of the cap 176 c as shown in FIG. 9A, and accordingly provides space between the conductor 180 c and at least one the electrodes 172 c. When an operator activates the probe 10 c (via, e.g., the button switch 124 c), the space between the electrodes 172 c and the conductor 180 c is effective for preventing at least a predetermined detectable amount of a low voltage current (e.g., 0.25 Volts) from being communicated between the electrodes via the conductor. Subsequently, when the operator abruptly forces the contact shield 196 c into contact with the patient's genital area, the shaft 188 c slides along the axis 208 c and thereby compresses the elastomeric component 200 c by an amount effective for causing the conductor 180 c to contact each of the spaced apart electrodes 176 c. Accordingly, the current flow between (and/or voltage change at) the electrodes 176 c can be detected for identifying a time indicative of the cap contacting the patient for inducing a BCR. Note that the cap 176 c may be configured to substantially guarantee that the cap is only used once by providing mating slanted teeth 212 c and 216 c (FIG. 10), respectively, on the interior of the bore 192 c and the shaft 188 c so that the shaft slides easily within the bore for compressing the elastomeric component 200 c, but does not (without substantial effort to the point of deforming the contact shield 196 c) move in the opposite direction. Moreover, by providing such mating slanted teeth, the elastomeric component 200 c may not be needed since these teeth alone may maintain the shaft and the conductor 180 c in a spaced apart relationship to the electrodes 172 c prior to use of the probe 10 c and its cap 176 c for inducing a BCR.

In another embodiment of the cap 176 c may include a flat spring 220 c provided along the shaft 188 c as shown in FIGS. 11 through 13, wherein when the cap 176 has not been used to contact a patient (e.g., the shaft 188 c is in its original position as in FIG. 9), the spring 220 c is folded against the shaft as shown in FIG. 12. However, once the cap 176 has been used to contact a patient (and accordingly, the shaft 188 c has been moved toward (or further into) the probe tip 34 c (FIG. 9)), the free side 224 c of the flat spring 220 c is no longer confined to the bore 192 c, and accordingly, expands away from the shaft 188 c as shown in FIGS. 11 and 13. Thus, the expanded free side 224 c of the spring 220 c prevents the shaft 188 c from being pulled back into its original position, and accordingly the cap 176 can be used only once. Note that one embodiment of the cap 176 c the mating slanted teeth may be unnecessary when the free side of the flat spring 22 c includes a bump 228 c for mating with a detent, divot, slot, or other in detention 232 c within the bore 192 c as illustrated in FIG. 14.

Another embodiment of the probe (10 d) and corresponding cap (176 d) is shown in FIGS. 15A and 15B, wherein components that functionally correspond to components of previous embodiments of the probe (10, 10 a, 10 b, 10 c) and the cap (176, 176 c) described hereinabove are identified by the same numerical label except with a “d” following. FIGS. 15A and 15B show cap 176 d for covering the probe tip 34 d, wherein this cap has a shaft 188 d which is slidable along axis 208 d within a bore 192 d through the cap 176 c. Fixedly attached to the shaft 188 d is an expanded portion 184 d (which may be a disk or a washer fixedly attached to the shaft), wherein the expanded portion is symmetric around the shaft 188 d, and the axis 208 d is also the axis of the shaft 188 d. A single electrical conductor 180 d (which may be a circular ring attached to the expanded portion 184 d, and concentric to the shaft 188 d) is provided. An outer end of the shaft 188 d is attached to a patient contact shield 196 d for contacting a patient's genital area and thereby inducing a BCR; the shield covers the tip 34 d, and according may be any of various shapes including hemispherical. An inner end of the shaft 188 d has attached thereto an elastomeric component 200 d such as a sponge-like material. The inner end of the shaft 188 d and the elastomeric component 200 d are received in a recess 204 d within the probe 10 d, wherein the shaft 188 d is slidable along the axis 208 c within the recess. Note that in the embodiment of FIGS. 15A and 15B, a piezoelectric disk (12 or 12 a) together with the pressure transferring components (e.g., the stimulus plunger (13 or 13 a), the compression spring (15 or 15 a), and the pressure transfer rod 78) of the probe embodiments 10 and 10 a are not needed in the present probe and cap combination. Moreover, by taking of the advantages of one or more of the improvements shown in FIGS. 10-14, of an identification chip (112) may not be needed for limiting the reuse of the cap 176 d.

During operation of the probe 10 d with the cap 176 d operably attached thereto as in FIGS. 15A and 15B, the elastomeric (or spring) component 200 d fits within the closed end of the recess 204 d and exerts a force effective for causing the expanded portion 184 d to contact the interior of the cap 176 d as shown in FIG. 15A. When the expanded portion 184 d contacts the interior of the cap 176 d as shown, the electrical conductor 180 d simultaneously contacts both the electrodes 172 d (each being represented by solid black squares in FIG. 15A). When an operator activates the probe 10 c (via, e.g., the button switch 124 c), a low voltage current (e.g., 0.25 Volts) is able to flow between the electrodes 172 d if the cap 176 d is properly fitted to the probe 10 d. Accordingly, an LED, or other light emitting device can provide the operator with positive feedback that the probe 10 d and cap 176 d are properly coupled for use. Upon forcefully and/or abruptly contacting a patient's genital area, the electrical conductor 180 d moves toward the tip 34 d, and accordingly slides past the electrodes 172 d so that the flow of current between the electrodes ceases. The detection of the cessation/reduction of current flow and/or the increase in voltage at one or more of the electrodes 172 d can provide a signal effective for commencing the timing of the delay in the (any) corresponding BCR. Note that, as with previous embodiments of the cap 176 d, it may be configured to substantially guarantee that the cap is only used once. In particular, the various techniques described hereinabove (e.g., slanted teeth, flat spring, etc.) may be also incorporated into the cap 176 d.

It is important to note that the techniques discussed above for substantially assuring that the patient contacting portion of the probe and/or a cap therefor are but one of many ways to prevent reuse with different patients.

The novel system and method disclosed herein is valuable in evaluation of urinary disorders in adults and children, as well as erectile dysfunction when neurological etiology is suspected. While various embodiments of the present disclosure have been described in detail, it will be apparent that further modifications and adaptations of the embodiment disclosed herein will occur to those skilled in the art. It is to be expressly understood that such modifications and adaptations are within the spirit and scope of the present disclosure. 

What is claimed is:
 1. A non-invasive method for measuring a bulbocavernosus reflex, comprising: providing a probe comprising: (i) a housing with a bore therethrough, said housing containing a piezoelectric disk, said disk electrically connected to an amplifier and activated by a power source; (ii) a stimulus plunger having first and second ends and having a shaft that extends through the bore, said shaft being movable along a longitudinal axis and having an expanded portion that prevents the stimulus plunger from sliding out of an opening in the housing; and (iii) a compression spring that biases said second end of the stimulus plunger away from contact with the piezoelectric disk; wherein when the probe is positioned so that a non-invasive contact of the stimulus plunger and a predetermined patient genital area occurs, the contact results in pressure from the stimulus plunger being transmitted to the genital area for inducing a bulbocavernosus reflex; activating the piezoelectric disk for the probe for generating an electromagnetic response indicative of the non-invasive contact; using the response to identify a collection of electrical responses from a plurality of electrodes placed on the patient's skin adjacent to the genital area, the collection being indicative of the bulbocavernosus reflex; outputting information representative of at least one of characteristics (a) through (d) following: (a) a time delay between the response and the collection are output with information, (b) a time duration for the collection, (c) a value indicative of a magnitude of at least one electrical response of the collection, and (d) an attenuation in the electrical responses of the collection; and wherein said method is employed to diagnose dysfunctions of spinal cord abnormalities.
 2. The method of claim 1, further including a step of determining each of the characteristics (a) through (d).
 3. The method as set forth in claim 1, wherein said piezoelectric disc comprises an electrical switch.
 4. The method as set forth in claim 1, further comprising determining a voltage difference between the plurality of electrodes.
 5. The method as set forth in claim 1, wherein said electrodes are placed on opposite sides of a patient's rectum.
 6. The method as set forth in claim 1, further comprising identifying a length of time a patient contacting portion has been activated by the probe.
 7. The method as set forth in claim 1, further comprising storing data indicative of a history of activation of the probe.
 8. A non-invasive method for measuring a bulbocavernosus reflex, comprising: providing a probe comprising: (i) a housing with a bore therethrough, said housing containing a piezoelectric disk, said disk electrically connected to an amplifier and activated by a power source; (ii) a stimulus plunger having first and second ends and having a shaft that extends through the bore, said shaft being movable along a longitudinal axis and having an expanded portion that prevents the stimulus plunger from sliding out of an opening in the housing; and (iii) a compression spring that biases said second end of the stimulus plunger away from contact with the piezoelectric disk; wherein when the probe is positioned so that a non-invasive contact of the stimulus plunger and a predetermined patient genital area occurs, the contact results in pressure from the stimulus plunger being transmitted to the genital area for inducing a bulbocavernosus reflex; activating the piezoelectric disk for the probe for generating an electromagnetic response indicative of the non-invasive contact; using the response to identify a collection of electrical responses from a plurality of electrodes placed on the patient's skin adjacent to the genital area, the collection being indicative of the bulbocavernosus reflex; outputting information representative of at least one of characteristics (a) through (d) following: (a) a time delay between the response and the collection are output with information, (b) a time duration for the collection, (c) a value indicative of a magnitude of at least one electrical response of the collection, and (d) an attenuation in the electrical responses of the collection; and wherein said method is employed to diagnose dysfunctions of bladder voiding.
 9. The method of claim 8, further including a step of determining each of the characteristics (a) through (d).
 10. The method as set forth in claim 8, wherein said piezoelectric disc comprises an electrical switch.
 11. The method as set forth in claim 8, further comprising determining a voltage difference between the plurality of electrodes.
 12. The method as set forth in claim 8, wherein said electrodes are placed on opposite sides of a patient's rectum.
 13. The method as set forth in claim 8, further comprising identifying a length of time a patient contacting portion has been activated by the probe.
 14. The method as set forth in claim 8, further comprising storing data indicative of a history of activation of the probe.
 15. A non-invasive method for measuring a bulbocavernosus reflex, comprising: providing a probe comprising: (i) a housing with a bore therethrough, said housing containing a piezoelectric disk, said disk electrically connected to an amplifier and activated by a power source; (ii) a stimulus plunger having first and second ends and having a shaft that extends through the bore, said shaft being movable along a longitudinal axis and having an expanded portion that prevents the stimulus plunger from sliding out of an opening in the housing; and (iii) a compression spring that biases said second end of the stimulus plunger away from contact with the piezoelectric disk; wherein when the probe is positioned so that a non-invasive contact of the stimulus plunger and a predetermined patient genital area occurs, the contact results in pressure from the stimulus plunger being transmitted to the genital area for inducing a bulbocavernosus reflex; activating the piezoelectric disk for the probe for generating an electromagnetic response indicative of the non-invasive contact; using the response to identify a collection of electrical responses from a plurality of electrodes placed on the patient's skin adjacent to the genital area, the collection being indicative of the bulbocavernosus reflex; outputting information representative of at least one of characteristics (a) through (d) following: (a) a time delay between the response and the collection are output with information, (b) a time duration for the collection, (c) a value indicative of a magnitude of at least one electrical response of the collection, and (d) an attenuation in the electrical responses of the collection; and wherein said method is employed to diagnose sexual organ dysfunctions.
 16. The method of claim 15, further including a step of determining each of the characteristics (a) through (d).
 17. The method as set forth in claim 15, wherein said piezoelectric disc comprises an electrical switch.
 18. The method as set forth in claim 15, further comprising determining a voltage difference between the plurality of electrodes.
 19. The method as set forth in claim 15, wherein said electrodes are placed on opposite sides of a patient's rectum.
 20. The method as set forth in claim 15, further comprising identifying a length of time a patient contacting portion has been activated by the probe. 